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Carbon Tetrachloride → N-(1-chloroethyl)-succinimide

HRID 2072362
Notes
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Reaction equation

HRID 2072362 reaction equation
[CH:1]([N:3]1[C:7](=[O:8])[CH2:6][CH2:5][C:4]1=[O:9])=[CH2:2].C(Cl)(Cl)(Cl)[Cl:11]>>[Cl:11][CH:1]([N:3]1[C:7](=[O:8])[CH2:6][CH2:5][C:4]1=[O:9])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 5943Carbon TetrachlorideHCID 219373N-Vinylsuccinimide

Product 1

HCID 12439633N-(1-chloroethyl)-succinimide

Procedure

N-vinylsuccinimide, 50.0 g. (0.40 mole) is dissolved in 1000 ml. carbon tetrachloride, 5.20 g. (0.020 mole) of stannic chloride is added and the mixture is stirred while saturating with hydrogen chloride for 6 hours at 20-30° C. After 24 hours, the mixture is resaturated with hydrogen chloride for 1.5 hours. At the end of 48 hours, the solution is decanted and the gummy residue is washed with ten 100 ml. portions of carbon tetrachloride. The combined extracts are slurried with 10 g. of diatomaceous earth, filtered an the filtrate concentrated under reduced pressure to approximately 400 ml. The N-(1-chloro-ethyl)-succinimide is filtered and dried at 20°-30° C. under reduced pressure to yield 38.4 g. (59%) of white solid melting at 83.5°-84.5° C.

Workup

  1. dissolution(0.40 mole) is dissolved in 1000 ml
  2. concentration
while saturating with hydrogen chloride for 6 hours at 20-30° C
  • waitthe mixture is resaturated with hydrogen chloride for 1.5 hours
  • customAt the end of 48 hours, the solution is decanted
  • washthe gummy residue is washed with ten 100 ml
  • filtrationof diatomaceous earth, filtered an the filtrate
  • concentrationconcentrated under reduced pressure to approximately 400 ml
  • filtrationThe N-(1-chloro-ethyl)-succinimide is filtered
  • customdried at 20°-30° C. under reduced pressure
  • customto yield 38.4 g
  • Sources & evidence

    ORD record
    ord-8b1d9cb1ce7341e1902728591f4e0ace
    Source dataset
    uspto-grants-1977_09
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04051169

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes